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Showing articles 0 to 10 of 10 Filter Applied: molecular genetics (Click to remove) Tuberous Sclerosis Lancet 372:657-658, Curatolo,P.,et al., 2008 The Tuberous Sclerosis Complex NEJM 355:1345-1356, Crino,P.B.,et al, 2006 New Developments in the Neurobiology of the Tuberous Sclerosis Complex Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999 Distal Myopathies:Clinical and Molecular Diagnosis and Classification JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients Ann Neurol 31:328-332, Yoshida,K.,et al, 1992 Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Showing articles 0 to 10 of 10